siRNA induced transcriptional gene silencing in mammalian cells

被引:57
作者
Kawasaki, H
Taira, K
Morris, KV
机构
[1] City Hope Natl Med Ctr, Beckman Res Inst, Div Mol Med, Duarte, CA 91010 USA
[2] Univ Tokyo, Sch Engn, Dept Chem & Biotechnol, Tokyo, Japan
[3] Natl Inst Adv Ind Sci & Technol, Gene Funct Res Ctr, Tsukuba, Japan
关键词
siRNA; transcriptional gene silencing; RNA mediated DNA methylation;
D O I
10.4161/cc.4.3.1520
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epigenetics is the study of meiotically and mitotically heritable changes in gene expression which are not coded for in the DNA.(1,2) Three distinct mechanisms appear to be intricately related and implicated in initiating and/or sustaining epigenetic modifications; DNA methylation, RNA-associated silencing, and histone modifications. 2 It has recently become clear in human cells that RNA plays a far more profound and complex role in regulating the expression of the gene. This regulatory effect is through RNA-associated silencing, can be transcriptional in nature, and is operable through an RNA interference based mechanism (RNAi) that is specifically mediated by small-interfering RNAs (siRNAs). Specifically, the recent observations by both our groups that siRNAs can silence target genes at the level of the chromatin in mammalian cells. We discuss here siRNA mediated transcriptional gene silencing and directed DNA methylation as well as the putative mechanism involved in human cells. Undoubtedly, the ramifications from this paradigm shift of RNA regulating the expression of the gene are immeasurable both therapeutically (i.e., directed control of a genes expression) and biologically in understanding the evolution of the cell.
引用
收藏
页码:442 / 448
页数:7
相关论文
共 74 条
[1]   Characterization of transgenic mice with targeted disruption of the catalytic domain of the double-stranded RNA-dependent protein kinase, PKR [J].
Abraham, N ;
Stojdl, DF ;
Duncan, PI ;
Méthot, N ;
Ishii, T ;
Dubé, M ;
Vanderhyden, BC ;
Atkins, HL ;
Gray, DA ;
McBurney, MW ;
Koromilas, AE ;
Brown, EG ;
Sonenberg, N ;
Bell, JC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (09) :5953-5962
[2]   RNA interference: Biology, mechanism, and applications [J].
Agrawal, N ;
Dasaradhi, PVN ;
Mohmmed, A ;
Malhotra, P ;
Bhatnagar, RK ;
Mukherjee, SK .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (04) :657-+
[3]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[4]   HDA6, a putative histone deacetylase needed to enhance DNA methylation induced by double-stranded RNA [J].
Aufsatz, W ;
Mette, MF ;
van der Winden, J ;
Matzke, M ;
Matzke, AJM .
EMBO JOURNAL, 2002, 21 (24) :6832-6841
[5]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[6]   Dicer is essential for mouse development [J].
Bernstein, E ;
Kim, SY ;
Carmell, MA ;
Murchison, EP ;
Alcorn, H ;
Li, MZ ;
Mills, AA ;
Elledge, SJ ;
Anderson, KV ;
Hannon, GJ .
NATURE GENETICS, 2003, 35 (03) :215-217
[7]   Role for a bidentate ribonuclease in the initiation step of RNA interference [J].
Bernstein, E ;
Caudy, AA ;
Hammond, SM ;
Hannon, GJ .
NATURE, 2001, 409 (6818) :363-366
[8]   The DNA methyltransferases of mammals [J].
Bestor, TH .
HUMAN MOLECULAR GENETICS, 2000, 9 (16) :2395-2402
[9]   DNA methylation patterns and epigenetic memory [J].
Bird, A .
GENES & DEVELOPMENT, 2002, 16 (01) :6-21
[10]   CPG ISLANDS AND GENES [J].
CROSS, SH ;
BIRD, AP .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1995, 5 (03) :309-314